Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.800 1.000 3 2006 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.020 1.000 2 2010 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.020 1.000 2 2010 2010
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
201 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.010 1.000 1 2014 2014
cardiac event
CUI: C0741923
Disease: cardiac event
18 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.010 1.000 1 2010 2010
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.010 1.000 1 2010 2010
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.010 1.000 1 2009 2009